The implant is designed for severe pathology associated with early onset scoliosis, according to a news release.
With breakthrough designation, the device’s development, assessment and review will be expedited.
OrthoPediatrics earns breakthrough designation for new scoliosis rod system
OrthoPediatrics earned the FDA’s breakthrough designation for the eLLi growing rod system for scoliosis, the devicemaker said May 2.
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SynerFuse is partnering with Velentium Medical to scale the SynerFuse e-TLIF implant, according to a March 21 news release. Velentium…
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Here are four spinal devices that have earned FDA approval, as reported by Becker’s since Jan. 24:
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